PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE— 510(k) K881378

Substantially Equivalent

Pfizer, Inc.

FDA 510(k) clearance K881378 for PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE, Substantially Equivalent on 1988-06-17. Applicant: Pfizer, Inc..

Clearance details

Applicant: Pfizer, Inc.
Product code: Code LXI
Advisory panel: General, Plastic Surgery
Date received: 1988-04-01
Decision date: 1988-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Groton, CT, US

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